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P Reynier

Showing results (101-110 of 106) with videos related to

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Human Reproduction (Oxford, England)|October 18, 2017
Targeted metabolomics reveals reduced levels of polyunsaturated choline plasmalogens and a smaller dimethylarginine/arginine ratio in the follicular fluid of patients with a diminished ovarian reserveJ M Chao de la Barca, T Boueilh, G Simard, et al.
Cell Death & Disease|August 14, 2015
AK2 deficiency compromises the mitochondrial energy metabolism required for differentiation of human neutrophil and lymphoid lineagesE Six, C Lagresle-Peyrou, S Susini, et al.
Molecular Genetics and Metabolism Reports|April 17, 2025
The recurrent p.Glu3Lys variant in <i>EHHADH</i> is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalitiesP Rollier, A Cospain, M Barth, et al.
Journal of Medical Genetics|September 3, 2004
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataractP Reynier, P Amati-Bonneau, C Verny, et al.
Cell Death Discovery|June 9, 2016
Loss of function of <i>Ywhah</i> in mice induces deafness and cochlear outer hair cells' degenerationL Buret, G Rebillard, E Brun, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Pageof 11

Showing results (101-110 of 106) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 106 results.
Human Reproduction (Oxford, England)|October 18, 2017
Targeted metabolomics reveals reduced levels of polyunsaturated choline plasmalogens and a smaller dimethylarginine/arginine ratio in the follicular fluid of patients with a diminished ovarian reserveJ M Chao de la Barca, T Boueilh, G Simard, et al.
Cell Death & Disease|August 14, 2015
AK2 deficiency compromises the mitochondrial energy metabolism required for differentiation of human neutrophil and lymphoid lineagesE Six, C Lagresle-Peyrou, S Susini, et al.
Molecular Genetics and Metabolism Reports|April 17, 2025
The recurrent p.Glu3Lys variant in <i>EHHADH</i> is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalitiesP Rollier, A Cospain, M Barth, et al.
Journal of Medical Genetics|September 3, 2004
OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataractP Reynier, P Amati-Bonneau, C Verny, et al.
Cell Death Discovery|June 9, 2016
Loss of function of <i>Ywhah</i> in mice induces deafness and cochlear outer hair cells' degenerationL Buret, G Rebillard, E Brun, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Pageof 11